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3.
J Child Neurol ; 25(8): 1017-9, 2010 Aug.
Artigo em Inglês | MEDLINE | ID: mdl-20110219

RESUMO

Posterior subcapsular cataract is a well-known complication of corticosteroid treatment. While this association has not been established for adrenocorticotropic hormone (ACTH) treatment, similar side effects would be expected for the 2 drugs given the mechanism of ACTH, which stimulates glucocorticoid synthesis and secretion. The authors report 2 children who were treated with ACTH for infantile spasms who developed bilateral posterior subcapsular cataracts. The authors recommend that children treated with ACTH be referred promptly to a pediatric ophthalmologist as these young, often developmentally delayed children may not exhibit recognizable signs of visual loss. Prompt evaluation and treatment of cataracts in children is important to prevent permanent vision loss from deprivation amblyopia.


Assuntos
Hormônio Adrenocorticotrópico/efeitos adversos , Catarata/induzido quimicamente , Catarata/patologia , Cristalino/efeitos dos fármacos , Cristalino/patologia , Espasmos Infantis/tratamento farmacológico , Hormônio Adrenocorticotrópico/uso terapêutico , Fatores Etários , Catarata/fisiopatologia , Pré-Escolar , Deficiências do Desenvolvimento/complicações , Deficiências do Desenvolvimento/patologia , Deficiências do Desenvolvimento/fisiopatologia , Feminino , Humanos , Lactente , Cristalino/crescimento & desenvolvimento , Espasmos Infantis/patologia , Espasmos Infantis/fisiopatologia
4.
J AAPOS ; 11(2): 162-5, 2007 Apr.
Artigo em Inglês | MEDLINE | ID: mdl-17306995

RESUMO

PURPOSE: To report 14 cases (28 eyes) of cataract associated with type-1 diabetes mellitus in young children and adolescents. METHODS: Retrospective review of the medical records of 14 patients from seven institutions. All patients under the age of 18 years who met the inclusion criteria of type-1 diabetes mellitus and cataract were included. RESULTS: Mean age at the time of diabetes diagnosis was 9.8 years (range, 0.5-14 years), and mean age at cataract diagnosis was 11.7 years (range, 5-16 years). Two patients presented with cataracts one month before the diagnosis of diabetes; seven after the diagnosis of diabetes; and in five patients the cataract was found at the time the diabetes was diagnosed by the pediatrician. Nineteen out of 23 operated eyes had a best corrected post operative visual acuity of 20/40 or better. Two patients (4 eyes) developed diabetic retinopathy postoperatively. CONCLUSIONS: Although cataract formation in type-1 diabetes is rare, it is treatable and potentially sight-saving in young children and adolescents.


Assuntos
Catarata/etiologia , Diabetes Mellitus Tipo 1/complicações , Adolescente , Extração de Catarata , Criança , Pré-Escolar , Feminino , Humanos , Implante de Lente Intraocular , Masculino , Estudos Retrospectivos , Acuidade Visual
5.
Ann Pharmacother ; 39(6): 1029-33, 2005 Jun.
Artigo em Inglês | MEDLINE | ID: mdl-15855243

RESUMO

BACKGROUND: Eye examinations for retinopathy of prematurity (ROP) are painful to the neonate. The use of topical anesthetic for eye examinations to evaluate ROP is routine in our neonatal intensive care unit (NICU), but does not completely suppress painful responses. Sweet solutions have been shown to reduce procedural pain in newborns. OBJECTIVE: To examine whether the addition of sucrose 24% to topical anesthetic improves procedural pain control during the ROP eye examination. METHODS: Neonates born at < or = 30 weeks' gestation were included in this placebo-controlled, double-blind, crossover study. Patients were randomly assigned to receive treatment with either proparacaine HCl ophthalmic solution 0.5% plus 2 mL of sucrose 24% or proparacaine HCl ophthalmic solution 0.5% plus 2 mL of sterile water (placebo) prior to an eye examination. In a subsequent eye examination, each patient received the alternate treatment. Oral sucrose and sterile water were prepared in the pharmacy in identical syringes, and physicians, nurses, and pharmacists in the NICU were blinded to the treatment given. Pain was measured using the Premature Infant Pain Profile (PIPP) scoring system, which measures both physical and physiologic measures of pain, and the scores were simultaneously assessed by 2 study nurses. PIPP scores were recorded 1 and 5 minutes before and after the eye examination and during initial placement of the eye speculum. The same ophthalmologist performed all eye examinations. Several different definitions of a pain response were investigated. RESULTS: Twenty-three infants were studied, with 12 receiving sucrose and 11 receiving placebo as the first treatment. For 3 of the 5 definitions of pain response, patients experienced significantly less pain at speculum insertion with sucrose than with placebo. After the ROP examination, pain responses were similar with either sucrose or placebo. CONCLUSIONS: Oral sucrose may reduce the immediate pain response in premature infants undergoing eye examination for ROP.


Assuntos
Dor/prevenção & controle , Retinopatia da Prematuridade/diagnóstico , Sacarose/uso terapêutico , Seleção Visual/métodos , Administração Oral , Anestésicos Locais/uso terapêutico , Estudos Cross-Over , Método Duplo-Cego , Quimioterapia Combinada , Idade Gestacional , Humanos , Recém-Nascido , Recém-Nascido Prematuro , Soluções Oftálmicas/administração & dosagem , Soluções Oftálmicas/uso terapêutico , Dor/tratamento farmacológico , Dor/etiologia , Medição da Dor/métodos , Propoxicaína/administração & dosagem , Propoxicaína/uso terapêutico , Retinopatia da Prematuridade/complicações , Sacarose/administração & dosagem , Fatores de Tempo , Resultado do Tratamento
6.
Ann Pharmacother ; 39(5): 829-33, 2005 May.
Artigo em Inglês | MEDLINE | ID: mdl-15797982

RESUMO

BACKGROUND: Eye examinations for retinopathy of prematurity (ROP) are stressful and probably painful, but many ophthalmologists do not apply topical anesthetics because their efficacy in reducing pain has not been established. OBJECTIVE: To evaluate the potential benefits of topical anesthetic eye drops in reducing pain during neonatal eye examination for ROP. METHODS: Neonates born at < or =30 weeks' gestation and expected to have at least 2 examinations for ROP were included. Patients were randomly assigned to receive either proparacaine HCl ophthalmic solution 0.5% or NaCl 0.9% (saline) eye drops prior to an eye examination. In a subsequent examination, each patient received the alternate treatment. Eye drops were prepared in the pharmacy in identical tuberculin syringes, and physicians, nurses, and pharmacists were blinded to the treatment given. Pain was measured using a scoring system with both physical and physiologic measures of pain (Premature Infant Pain Profile [PIPP], possible range 1-21), which has been validated in preterm infants. PIPP scoring was performed simultaneously by 2 nurses: 1 and 5 minutes before and after the eye examination and during initial placement of the eye speculum. The same ophthalmologist performed all examinations. RESULTS: Twenty-two patients were studied, with 11 infants receiving proparacaine and 11 receiving saline as the first treatment. Crossover was performed with a median of 17.5 days between treatments. Patients experienced significantly less pain at speculum insertion with proparacaine than with saline (paired difference -2.5 +/- 3.4; p = 0.001). CONCLUSIONS: Topical anesthetic pretreatment reduces the pain response to eye examination for ROP and should become routine practice. Because this is not effective in all infants, additional measures to reduce pain should be taken.


Assuntos
Anestésicos Locais , Medição da Dor/métodos , Dor/tratamento farmacológico , Propoxicaína , Retinopatia da Prematuridade/diagnóstico , Administração Tópica , Estudos Cross-Over , Técnicas de Diagnóstico Oftalmológico , Método Duplo-Cego , Humanos , Recém-Nascido , Recém-Nascido Prematuro , Unidades de Terapia Intensiva Neonatal , Triagem Neonatal , Dor/classificação
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